{
    "disease_id": "DOID:0070524",
    "recommended_name": {
        "id": "DOID:0070524",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0070524",
        "name": "peeling skin syndrome 5",
        "description": "A peeling skin syndrome that has_material_basis_in homozygous mutation in the SERPINB8 gene on chromosome 18q22.1."
    },
    "synonyms": [
        {
            "id": "DOID:0070524",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0070524",
            "name": "PSS5",
            "description": ""
        },
        {
            "id": "MONDO:0014923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014923",
            "name": "peeling skin syndrome 5",
            "description": "Any peeling skin syndrome in which the cause of the disease is a mutation in the SERPINB8 gene."
        },
        {
            "id": "MONDO:0014923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014923",
            "name": "PSS5",
            "description": ""
        },
        {
            "id": "MONDO:0014923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014923",
            "name": "SERPINB8 peeling skin syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0014923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014923",
            "name": "peeling skin syndrome 5",
            "description": ""
        },
        {
            "id": "MONDO:0014923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014923",
            "name": "peeling skin syndrome 5; PSS5",
            "description": ""
        },
        {
            "id": "MONDO:0014923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014923",
            "name": "peeling skin syndrome caused by mutation in SERPINB8",
            "description": ""
        },
        {
            "id": "MONDO:0014923",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014923",
            "name": "peeling skin syndrome type 5",
            "description": ""
        },
        {
            "id": "MIM:617115",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/617115",
            "name": "Peeling skin syndrome 5",
            "description": "Peeling skin syndrome 5"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0070524"
    ],
    "unlinked_id_list": []
}